(3S,5S,11R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-S-METHYL-1-CYSTEINE
Compound with spectra: 1 NMR
![(3S,5S,11R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-S-METHYL-1-CYSTEINE](/api/compound/LCu802VlG6o.png?ph=true&h=300&w=458 "(3S,5S,11R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-S-METHYL-1-CYSTEINE")
| SpectraBase Compound ID | LCu802VlG6o |
|---|---|
| InChI | InChI=1S/C14H19NO5S.Na/c1-4-9-5-10(6-12(16)8(9)2)20-14(19)15-11(7-21-3)13(17)18;/h1,10-12,16H,5-7H2,2-3H3,(H,15,19)(H,17,18);/q;+1/p-1/t10-,11-,12+;/m0./s1 |
| InChIKey | VDUGTZWKBOWIFL-AHBISNNASA-M |
| Mol Weight | 335.35 g/mol |
| Molecular Formula | C14H18NNaO5S |
| Exact Mass | 335.080338 g/mol |
| Parent InChIKey | IPYHJSMKOHLEAK-SDDRHHMPSA-M |
| Enantiomer InChIKey | VDUGTZWKBOWIFL-HSASPSRMSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(3S,5R)/(3R,5R)-3,5-DIACETOXY-1-ETHYNYL-2-METHYLCYCLOHEX-1-ENE
(3R,5R)-3-[(Acetonoxime)carbonyloxy]-1-ethynyl-5-hydroxy-2-methyl-1-cyclohexene
2-[1-[[(2R)-2-(tert-butoxycarbonylamino)-3-keto-3-methoxy-propyl]thio]-1-methyl-ethyl]malonic acid diethyl ester
[(2R)-N-(TERT.-BUTOXYCARBONYL)-ALPHA-METHYLASPARTYL]-BETA-(2S)-PHENYLALANYL-ESTER
N-ALPHA-(2-PHENYLISOPROPYLOXYCARBONYL)-O-(DIBENZYLPHOSPHONO)-L-SERINE;PPOC-SER(PO3BZL2)-OH
CUFRCAJZKAEERP-UHFFFAOYSA-N
(phenylmethyl) 2-[[2-(phenylmethoxycarbonylamino)-3-(phenylmethylsulfanyl)propanoyl]amino]propanoate
(R)-3-BENZYLOXYCARBONYL-4-(ACETYLTHIOMETHYL)-OXAZOLIDIN-5-ONE
acetic acid [4-[(E)-3-ketobut-1-enyl]-3,5,5-trimethyl-1-cyclohex-3-enyl] ester
(-)-Harveynone
| Title | Journal or Book | Year |
|---|---|---|
| Selective Alkoxycarbonylation of A-Ring Precursors of Vitamin D Using Enzymes in Organic Solvents. Chemoenzymatic Synthesis of 1α,25-Dihydroxyvitamin D3 C-5 A-Ring Carbamate Derivatives1 | The Journal of Organic Chemistry | 1997 |